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CISD2 gene

Known as: NUTRIENT DEPRIVATION AUTOPHAGY FACTOR 1, nutrient-deprivation autophagy factor-1, ENDOPLASMIC RETICULUM INTERMEMBRANE SMALL PROTEIN 
This gene plays a role in the regulation of autophagy.
National Institutes of Health

Papers overview

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2018
2018
Sulfasalazine has been repurposed to induce ferroptotic cancer cell death via inhibition of xc--cystine/glutamate antiporter (xCT… Expand
Highly Cited
2014
Highly Cited
2014
CISD2 is a causative gene associated with Wolfram syndrome (WFS). However, it remains a mystery as to how the loss of CISD2… Expand
Highly Cited
2013
Highly Cited
2013
Mitochondria are emerging as important players in the transformation process of cells, maintaining the biosynthetic and energetic… Expand
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Highly Cited
2012
Highly Cited
2012
To extend understanding of the genetic architecture and molecular basis of type 2 diabetes (T2D), we conducted a meta-analysis of… Expand
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Highly Cited
2012
Highly Cited
2012
The CISD2 gene, which is an evolutionarily conserved novel gene, encodes a transmembrane protein primarily associated with the… Expand
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Highly Cited
2010
Highly Cited
2010
Although the essential genes for autophagy (Atg) have been identified, the molecular mechanisms through which Atg proteins… Expand
2010
2010
Human mitoNEET is a homodimeric iron-sulfur protein located in the outer mitochondrial membrane with unknown function, but which… Expand
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Highly Cited
2009
Highly Cited
2009
CISD2, the causative gene for Wolfram syndrome 2 (WFS2), is a previously uncharacterized novel gene. Significantly, the CISD2… Expand
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Highly Cited
2009
Highly Cited
2009
The endoplasmic reticulum protein Miner1 is essential for health and longevity. Mis-splicing of CISD2, which codes for Miner1, is… Expand
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Highly Cited
2007
Highly Cited
2007
A single missense mutation was identified in a novel, highly conserved zinc-finger gene, ZCD2, in three consanguineous families… Expand